Our study co-led by @gretapinta, @flassen_, @yuhanhsu and @mjapkim, ‘Genoppi: an open-source software for robust and standardized integration of proteomic and genetic data’, is now posted as a pre-print on bioRxiv. Genoppi allows the seamless integration of proteomic data with genetic information from a multitude of public or custom gene lists to maximize the interpretation of protein interaction datasets.
Nadine’s paper on identification of new biomarkers for IBD published in Nature Microbiology
Nadine’s work on identification of new biomarkers of Inflammatory Bowel Disease (IBD), under the direction of Ramnik Xavier in collaboration with the Broad Institute, Harvard School of Public Health, the University of North Carolina and Novartis has been published in Nature Microbiology. Fantastic work Nadine!
Find the digest here: https://naturemicrobiologycommunity.nature.com/users/346662-nadine-fornelos/posts/58611-gut-bugs-and-metabolites.
Find the article here: https://www.nature.com/articles/s41564-019-0655-7

BINe team hosts the Stanley Center February Social
The Brain Interaction Network (BINe) team hosted the February Stanley Center Social and introduced its people to the Stanley Center community.
Taibo Li awarded full MD/PhD scholarship from Johns Hopkins School of Medicine
Taibo has recently been awarded a full MD/PhD scholarship to Johns Hopkins School of Medicine. Taibo started in the Lage Lab in April 2013 and worked on several projects including InWeb, GeNets, BINe, CanComSq. He looks forward to continuing working with the Lage Lab from his new position at Hopkins and we wish him the best of luck!
April Kim and Edyta Malolepsza host BroadE workshop on web platform Genoppi that integrates experimental proteomics and genetic data
April Kim presents GeNets at Boot Camp for new postdocs joining the Broad Institute’s Cancer Program
Kasper and April were invited by Brett Tomson to present GeNets as part of the network tools lecture to the postdocs attending Cancer Program BootCamp.
April Kim and Edyta Malolepsza presents CanComSq and showcase Genoppi at Boot Camp for new postdocs joining the Broad Institute’s Cancer Program
Jakob Jespersen presented his work at the Center for Mendelian Genetics at the Broad Institute
Jakob Jespersen, member of Lage Lab at MGH and the Broad Institute, presented at the Center for Mendelian Genetics Analysis meeting the Interpretation of missense variants using protein structures and features. Jakob explained that with a vast amount of exome sequencing data, it is difficult to identify the missense variants that may be implicated in diseases. While it is possible to crudely classify variants as “loss of function” based on observations such as the mutation being in a splice site, creating a stop codon or frameshift, it is much more difficult to determine whether missense mutations are deleterious or benign.
Since the Protein Data Bank (PDB) hosts information on more than 6,000 different human proteins, it is possible to add structural information to help the classification of missense mutations. Some methods are already utilizing features from 3D protein structures, so the presentation was focused on features that we can extract and calculate which are not in use yet as well as a computational tool set Jakob has developed for this purpose.
Enjoy the recording of the Jakob’s presentation in the video below (Sep 20th, 2016)
Taibo Li gave an invited poster presentation at the Fourth Annual Broad Institute – Israel Science Foundation Cell Circuits Symposium
The title of his poster ‘Human brain networks perturbed by genetics and targeted by therapeutics in psychiatric disorders’
Joy Poulo Presented his work at a Simches Seminar at MGH
Title of Joy’s talk: “Congenital Diaphragmatic Hernia: Exome sequence analysis of trios”


